Skuza Grazyna
Department of Pharmacology, Institute of Pharmacology, Polish Academy of Sciences, Smetna 12, PL 31-343 Kraków, Poland.
Pol J Pharmacol. 2003 Nov-Dec;55(6):923-34.
Despite many years' studies of antidepressant drugs (ADs), their mechanism of action still remains unclear. Recently, it has been postulated that substances capable of reducing neurotransmission at the NMDA complex may represent a new class of ADs. Since several ADs have a high affinity for sigma receptors, the sigma binding site may be a relevant mechanism in antidepressant action. Moreover, sigma ligands are able to modulate the activity of the central neurotransmitter systems, including noradrenergic, serotonergic, dopaminergic and glutamatergic (NMDA) ones, which are seemingly important for the mechanism of action of known ADs. The existence of at least two different subtypes of sigma receptors, denoted sigma1 and sigma2 is now widely accepted. The selective agonists of both sigma receptor subtypes are available at present. In particular, a potential antidepressant activity of sigma1 receptor agonists has been postulated, since the antidepressive-like actions of these compounds have been shown in animal models. This article reviews the findings related to potential antidepressant activity of new, selective sigma ligands.
尽管对抗抑郁药物(ADs)进行了多年研究,但其作用机制仍不清楚。最近,有人提出能够降低NMDA复合体神经传递的物质可能代表一类新型抗抑郁药物。由于几种抗抑郁药物对σ受体具有高亲和力,σ结合位点可能是抗抑郁作用的一个相关机制。此外,σ配体能够调节中枢神经递质系统的活性,包括去甲肾上腺素能、血清素能、多巴胺能和谷氨酸能(NMDA)系统,这些系统似乎对已知抗抑郁药物的作用机制很重要。现在人们广泛接受至少存在两种不同亚型的σ受体,分别称为σ1和σ2。目前已有两种σ受体亚型的选择性激动剂。特别是,有人推测σ1受体激动剂具有潜在的抗抑郁活性,因为这些化合物在动物模型中已显示出类似抗抑郁的作用。本文综述了与新型选择性σ配体潜在抗抑郁活性相关的研究结果。